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480 citation(s) found for "Pittock, S J".

Disability profile of MS did not change over 10 years in a population-based prevalence cohort
Pittock, Sean J. , Mayr, William T., McClelland, Robyn L. , Jorgensen, Neal W. , Weigand, Stephen D. , Noseworthy, John H., Rodriguez, Moses , Pittock, S J

Mayo Clinic

Neurology | May 13, 2012 | Volume: 62 | Issue: 4 | Pages: 601-606

10.1212/wnl.62.4.601 | PMID 14981177 Get It

Change in MS-related disability in a population-based cohort
Pittock, Sean J. , Mayr, William T., McClelland, Robyn L. , Jorgensen, Neal W. , Weigand, Stephen D. , Noseworthy, John H., Weinshenker, Brian G. , Rodriguez, Moses , Pittock, S J , Weinshenker, Brian G

Mayo Clinic

Neurology | May 13, 2012 | Volume: 62 | Issue: 1 | Pages: 51-59

10.1212/01.wnl.0000101724.93433.00 | PMID 14718697 Get It

Incidence and prevalence of multiple sclerosis in Olmsted County, Minnesota, 1985–2000
Mayr, William T., Pittock, Sean J. , McClelland, Robyn L. , Jorgensen, Neal W. , Noseworthy, John H., Rodriguez, Moses , Pittock, S J

Mayo Clinic

Neurology | May 13, 2012 | Volume: 61 | Issue: 10 | Pages: 1373-1377

10.1212/01.wnl.0000094316.90240.eb | PMID 14638958 Get It

Emerging synaptic biomarkers in autoimmune dementia
Pittock, Sean J. , Balice‐Gordon, Rita J. , Pittock, S J

Mayo Clinic

Neurology | April 27, 2012 | Volume: 78 | Issue: 22 | Pages: 1710-1711

10.1212/wnl.0b013e31825830f3 | PMID 22539567 Get It

Do not treat from CIS onset: evaluate disease course and prognosis first – Yes
Bunyan, Reem F., Pittock, Sean J. , Pittock, S J

Mayo Clinic

Multiple Sclerosis Journal | April 3, 2012 | Volume: 18 | Issue: 4 | Pages: 391-393

10.1177/1352458512440604 | PMID 22473500 Get It

As physicians how do we counsel our patients with clinically isolated syndrome (CIS) when they ask, ‘what is the benefit of injecting disease-modifying agents (DMAs) over many years? What disability will they prevent in my future?’ In this debate, we will provide three core points supporting the concept that a watchful waiting approach (annual neurological evaluation and magnetic resonance imaging of the head (with gadolinium) at least for the first few years after diagnosis) for most patients with CIS represents appropriate medical care.
Syndrome of inappropriate antidiuresis may herald or accompany neuromyelitis optica
Iorio, Raffaele , Lucchinetti, Claudia F. , Lennon, Vanda A. , Costanzi, Chiara, Hinson, Shannon R., Weinshenker, Brian G. , Pittock, Sean J. , Pittock, S J , Weinshenker, Brian G , Iorio, Raffaele

Mayo Clinic

Neurology | October 14, 2011 | Volume: 77 | Issue: 17 | Pages: 1644-1646

10.1212/wnl.0b013e3182343377 | PMID 21998320 Get It

Statin therapy and multiple sclerosis disability in a population-based cohort
Soldán, M. Mateo Paz , Pittock, Sean J. , Weigand, Stephen D. , Yawn, Barbara P. , Rodriguez, Moses , Pittock, S J , Rodriguez, Moses , Paz Soldán, M Mateo

Mayo Clinic

Multiple Sclerosis Journal | September 9, 2011 | Volume: 18 | Issue: 3 | Pages: 358-363

10.1177/1352458511421920 | PMID 21908483 Get It

Background: Axonal damage and inflammatory demyelination both occur in multiple sclerosis (MS). Some studies suggest that statins, through pleiotropic effects, reduce inflammatory episodes and protect neurons. However, other studies suggest statins have disparate impacts on these pathologic processes. Objective: The objective of this study was to assess disability progression in MS patients receiving statin therapy. Methods: We performed a retrospective medical record review of an established population-based MS prevalence cohort in Olmsted County, Minnesota, comparing disability progression between patients receiving statins and controls. Results: Duration of statin use ranged from 1.9 to 20.3 years with a mean and standard deviation of 6.8 ± 4 years. Years between assessments ranged from 0.6 to 8.2 (75% of patients having intervals >6.4 years). The median (interquartile range) absolute change of disability among the statin group was 0 (0 to +1), compared with +0.5 (0, +1) in the no-statin group. Distributions were not significantly different ( p = 0.39). The mean (standard deviation) absolute change of disability scores among the statin group was +0.69 (+1.49), not significantly different from +0.61 (+1.31) in the no-statin group. Likewise, annualized disability scores did not differ significantly ( p = 0.23). Eighteen (40%) patients worsened by 1.0 or more on Expanded Disability Status Scale (EDSS) in the statin group and 36 (40%) in the no-statin group ( p = 0.85, chi-squared test). Conclusions: In this cohort, disability progression did not differ between those receiving statin therapy and controls. These findings support the hypothesis that statins, in doses currently prescribed for hyperlipidemia, do not affect the long-term course of MS.